US2658876A - Diazo thioethers as blowing agents in production of sponge rubber and the like - Google Patents

Diazo thioethers as blowing agents in production of sponge rubber and the like Download PDF

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US2658876A
US2658876A US28280A US2828048A US2658876A US 2658876 A US2658876 A US 2658876A US 28280 A US28280 A US 28280A US 2828048 A US2828048 A US 2828048A US 2658876 A US2658876 A US 2658876A
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diazo
rubber
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thioether
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William B Reynolds
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Phillips Petroleum Co
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/06Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent
    • C08J9/10Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent developing nitrogen, the blowing agent being a compound containing a nitrogen-to-nitrogen bond
    • C08J9/102Azo-compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L21/00Compositions of unspecified rubbers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2321/00Characterised by the use of unspecified rubbers

Definitions

  • This invention relates to sponge, foam, or cellularrubber, any of which can bereferred to as blown rubber.
  • the invention also relates to a new process for producing sponge, foam, or cellular,- or blown, rubber.
  • sodium bicarbonate is commonly employed, its chief advantages being its availability and low cost, but it fails to meet many of the requirements of agood sponging or blowing agent. Uniform dispersion of sodium bicarbonate in the rubber is difiicult to attain and the product whichresults has uneven, coarse cells. Ammonium carbonate has also been employed vin the production of sponge rubber. It is more drastic in its action than sodium bicarbonate and exerts a high pressure when heated but its tendency "to reform on cooling may cause the collapse of, the cellular structure.
  • One object of this invention is to produce sponge, foam, andcellular rubber.
  • a further object'of this invention is to blow rubber.
  • Another object of this invention is to provide a method for the production of sponge rubber from natural rubber.
  • a further object of this invention is to provide a method for the production of sponge rubber f-romsynthetic rubber.
  • Another object of this invention is to expand, and produce foam rubber from, a rubber latex; Still another object of thisinvention to produce a sponge, foam, or cellular, rubber of uniform pore size.
  • mula RN NS-R', whereB. is an aromatic radical and R is a member of the group consisting of the aromatic, cycloalkyl, and aliphatic radicals.
  • diazo thioethers may be madeqby 'thecombination of a diazotized aromatic amine and an aromatic, .cycloalkyl or aliphatic mercaptan, including substituted derivatives thereof.
  • Preferred .substituent groups are the alkyl, alkoxy, aryloxy .(e. g., phenoxy), .carboxy, sulfo (SOsH).
  • blowing agents .used in this invention comprise the following, the list being primarily illustrative, but not unduly limiting to'the scope .of the invention: 2-(4.-me,thoxybenzene diazo mercapto) --naphthalene, 1 -'(4- methoxybenzene diazo.
  • the diazo thioether blowing agents are applicable in either natural or synthetic rubber stocks to producesponge rubber, and they may also .be employed in latex, either natural or synthetic, to produce foam rubber.
  • rubbertin includes'both naturaland'synthetic rubbers and the term latex includes both --natu-ral and' synthetic" latices.
  • the diazo .thioethers may be introduced by any -con-' ventional method. For example, they may be dissolved inany suitable solvent, such as benzene,
  • the amount of blowing .agent may be :varied, depending .upon the particular diazo thioether usedas .well as upon the amount of blow desired. Larger proportions of theadditive :are introduced in;instances .where a .greater amount of blow' is desired. In general, a relatively small proportion of diazo thioether is used, c. g., 0.5 to per cent of the rubber stock, preferably 1.5 to 5 per cent, but larger amounts may be added in cases where it is advantageous to do so.
  • the diazo thioether is generally incorporated uniformly in the rubber, or latex, to be blown.
  • the mixture is heated, usually in a chosen with these factors in mind.
  • a suitable temperature for this step of the process will generally be found between 90 and 200 C.
  • the heating should be for a time between 5 and 69 minutes, preferably 29 to 30 minutes.
  • heating of the compounded mixture is carried out with the mixture in a mold the mold is usually only partially filled, e. g. about one-third to one-half full of the mixture. If a latex is me- When such 1 chanically frothed, to include small bubbles of air or other gas, such a froth may be used to fill the mold completely.
  • a further advantage of the use of a diazo thioether as a blowing agent in the process of this are vulcanization accelerators, and hence perform that function in addition to their role as blowing agents. The necessity of using additiona1 accelerators is thus eliminated.
  • Diazo thioethers are also employed as initiators and modifiers in polymerization recipes,in the production of synthetic rubber. When synthetic rubber is produced from formulations in which diazo thioethers are employed, the diazo thioether already present may serve as a blowing agent in the manufacture of foam or sponge rubber, if it is present, as such, in the final polymer product in sufficient relative amount. In cases where an additional amount of this additive is considered desirable, such quantities as are necessary may be introduced prior to the blowing operation.
  • the diazo thioether blowing agent may be admixed with raw rubber, without or with the concomitant admixture of other ingredients. This procedure can be used, for example, when nonvulcanizable synthetic rubber is to be blown. However, it is generally preferable to effect vulcanization of the rubber at the same time, and in invention lies in the fact that diazo thioethers such cases there is added, along with the diazo i 3 thioether blowing agent, the other ingredients which it is desired to incorporate in the rubber. In these instances, blowing and vulcanization oc cur together and the resulting sponge, foam, or cellular rubber product is also a vulcanized product.
  • diazo thioethers are vulcanization accelerators also, usual accelerators may be omitted, or used in less-than-normal amount.
  • a diazo thioether is used in very small concentration, its eflect as a vulcanization accelerator may exceed its effect as a blowing agent.
  • GR-S rubber stock Santocure 1 0.5 Calcined magnesia 4 Whiting 60 Carbon blackiPhilblack A) 15 Phenyl-beta-naphthylamine 2 Petroleum softener 20 Stearic acid r 2 Zinc oxide 5 '2- l-methoxybenzene diazo mercapto) naphthalene 3 1 N-cyclohexyl-2-benzothiazole sulfenamide.
  • a firm sponge is prepared from a GR-S rubber stock by using the following compounding recipe:
  • Example IV A natural rubber base stock-iscompounded according to the f'ollowingrecipe:
  • Foam rubber is prepared from -a sample of GR-S latex which is mechanically frothed, by intimatemixing with air, to about six times. its original volume and then admixed with a material comprising compounding, blowing, gelling, and vulcanizing ingredients. This latter material is prepared in the following manner:
  • Phenyl-beta-naphthylamine 5 Piperidinium pentamethylene dithiocarbamate 4.5 Zinc oxide 20 Sulfur 10 Zinc mercaptobenzothiazole 5.5 Agerite white 6 1 Di-beta-naphthyl-para-phenylene diamine.
  • the water is heated to 80 to 85 C'., the phenylbeta-naphthylamine and piperidinium pentamethylene dithiocarbamate added, and the mixture placed in a ball mill after which the zinc oxide, sulfur, zinc mercaptobenzothiazole, and agerite white are introduced.
  • the ingredients are milled until a uniform paste is obtained.
  • the ball mill is filled to maximum capacity.
  • To 100 parts of the paste is added parts of the sodium salt of 4-(4-sulfobenzene diazo mercapto)-toluene and 2.5 parts ammonium nitrate in the form of a 50 per cent aqueous solution. This mixture is stirred until a uniform dispersion is produced.
  • the compounding mixture prepared as described (2 parts) is added to 10 parts of latex frothed to about six times its original volume, and this mixture is poured into a mold which h'as been warmed to a temperature of 65 C. l
  • the temperature. is increased to -90 C. to hasten gelling of the. latex and cause thefrothed rubber to expand and fill the mold completely.
  • the slight pressure, caused by the freed gases, maintained until a-stiif gel is produced: after which the latex is vulcanized by heating the mold to.100 C.for about an hour.
  • TheGR-S rubber stock referred to some of the foregoing examples is, as is well known to thoseskil-ledin the art, asynthetic rubber producedby emulsion copolymerization of a meme meric mixture of 1,3-butadiene (70-75%) and styrene (25-30%).
  • This material was produced in. large quantities under government direction by'many organizations.
  • various modifications of this invention can be made, orfollowed, in the light of the foregoing disclosure and discussion, without departing from the spirit or scope of the disclosure or from the scope of the claims. h
  • a process according to claim 3 wherein the quantity of the diazo thioether incorporated is in the approximate range 0.5 to 10% by weight of the rubber in said latex and the admixture is heated to a temperature in the approximate range to 200 C. to cause the decomposition of said diazo thioether and for a time sufiicient to cause the formation of said product, said agent having the general formula R.-N NS-R', wherein R is an aromatic radical and R is a member of the group consisting of aromatic, cycloalkyl and aliphatic radicals.
  • a froth is first formed by admixing a gas with said latex.
  • a process according to claim 1 wherein said diazo thioether is 2-(4-methoxybenzene diazo mercapto) -naphthalene.
  • diazo thioether is 1-(4-methoxybenzene diazo mercapto) -naphthalene.
  • diazo thioether is a 2,4-dimethylbenzene diazo mercapto-napthalene.
  • diazo thioether is 2-(2,4-dimethylbenzene diazo mercapto) -naphthalene.
  • a process according to claim 1 wherein said diazo thioether is 2-(4-methylbenzene diazo mercapto) -naphthalene.

Description

Patented Nov. 10, 1953 DIAZO ITHIOE'IQHEBS AS BLOWING AGENTS IN PRODUCTION-F SPONGE RUBBER AND THE LIKE William B. Reynolds, Bartlesville, 0kla., assignor to Phillips Petroleum Company, a corporation of Delaware No Drawing. Application May 20, 1948, Serial No. 28,280
(01. zoo -2.5)
This invention relates to sponge, foam, or cellularrubber, any of which can bereferred to as blown rubber. The invention also relates to a new process for producing sponge, foam, or cellular,- or blown, rubber.
Numerous methods have been employed for the production of sponge rubber, one of which involves incorporating into the rubber a material which'will decompose when subjected to heat,
thereby l-iberatinga gas which will cause the rubber to expand and assume a cellular form. Among the agents .used in this capacity, known as sponging agen or blowing agents", sodium bicarbonate is commonly employed, its chief advantages being its availability and low cost, but it fails to meet many of the requirements of agood sponging or blowing agent. Uniform dispersion of sodium bicarbonate in the rubber is difiicult to attain and the product whichresults has uneven, coarse cells. Ammonium carbonate has also been employed vin the production of sponge rubber. It is more drastic in its action than sodium bicarbonate and exerts a high pressure when heated but its tendency "to reform on cooling may cause the collapse of, the cellular structure.
I have now found a method whereby sponge rubber of uniform pore size and finetexture may be produced through the use of diazo thioethers as "blowing agents. The-blowing agents'used in this invention impart :alhigh :ratio aofuexpansion to the rubber, .are readily incorporated into the rubber to give a uniform dispersion, and will provide firm products which are .not harsh to the touch.
One object of this invention is to produce sponge, foam, andcellular rubber.
A further object'of this invention is to blow rubber.
Another object of this invention is to provide a method for the production of sponge rubber from natural rubber.
A further object of this invention is to provide a method for the production of sponge rubber f-romsynthetic rubber.
, Another object of this invention is to expand, and produce foam rubber from, a rubber latex; Still another object of thisinvention to produce a sponge, foam, or cellular, rubber of uniform pore size.
A still further object of ,myinventionistoproduce a sponge, foam, or cellular rubber pf1fine texture.
7 Further objects and advantages .ofmy invention will become apparent, to-oneskilledm the art, from the accompanying disclosure and discussion.
ixThe diazo thioethers', used in the practice :of this invention, have the. general structural .for-
mula RN=NS-R', whereB. is an aromatic radical and R is a member of the group consisting of the aromatic, cycloalkyl, and aliphatic radicals. These diazo thioethers may be madeqby 'thecombination of a diazotized aromatic amine and an aromatic, .cycloalkyl or aliphatic mercaptan, including substituted derivatives thereof. Preferred .substituent groups are the alkyl, alkoxy, aryloxy .(e. g., phenoxy), .carboxy, sulfo (SOsH). halo, and nitro groups, It is to be understood that such substituent groups may be present in R and/or R in the above general formula. It is also. to be understood that this invention is not concerned with the preparation of diazo thioethers and is not limited to any particular method of synthesis but pertains 1301131181186 of :these materials as blowing agents in sponge rubber manufacture.
Typical examples of blowing agents .used in this invention comprise the following, the list being primarily illustrative, but not unduly limiting to'the scope .of the invention: 2-(4.-me,thoxybenzene diazo mercapto) --naphthalene, 1 -'(4- methoxybenzene diazo. 'mercaptm-naphthalene, 2-'(2,4-dimethylbenzene diazo mercaptol-maphthalene, 1-2,!1-.dimethylbenzene diazo mercapto) -naphthalene, 4-(2,4-dimethylbenzene diazo mercapto) naphthalene, sodium salt of .2- L methoxybenzene diazo mercaptol-benzoic acid. sodium salt of 2 (4 --sulfobenzene diazo mercaptoi-naphthalene. sodium salt of 4-;t4-rsulfobenzenediazo merca-pto) -toluene, sodium ;salt of 2-(2-naphthalene diazo mercapto) -benzoic acid. and the like. Usually .only one diazo thioether will vbe used at any onetime, but mixtures of such .thioethers may .be used, when desirable or expedient. V
The diazo thioether blowing agents are applicable in either natural or synthetic rubber stocks to producesponge rubber, and they may also .be employed in latex, either natural or synthetic, to produce foam rubber. Herein and in theclaims-the term rubbertincludes'both naturaland'synthetic rubbers and the term latex includes both --natu-ral and' synthetic" latices. The diazo .thioethers may be introduced by any -con-' ventional method. For example, they may be dissolved inany suitable solvent, such as benzene,
and added to the latex or they may 'beincor porated .into the rubber composition on a mill;
They are applicable numerous compounding recipes-land may be employedin either the pres ence or absence of carbon black.
The amount of blowing .agent may be :varied, depending .upon the particular diazo thioether usedas .well as upon the amount of blow desired. Larger proportions of theadditive :are introduced in;instances .where a .greater amount of blow' is desired. In general, a relatively small proportion of diazo thioether is used, c. g., 0.5 to per cent of the rubber stock, preferably 1.5 to 5 per cent, but larger amounts may be added in cases where it is advantageous to do so. The diazo thioether is generally incorporated uniformly in the rubber, or latex, to be blown.
Thereafter the mixture is heated, usually in a chosen with these factors in mind. A suitable temperature for this step of the process will generally be found between 90 and 200 C. The heating should be for a time between 5 and 69 minutes, preferably 29 to 30 minutes. heating of the compounded mixture is carried out with the mixture in a mold the mold is usually only partially filled, e. g. about one-third to one-half full of the mixture. If a latex is me- When such 1 chanically frothed, to include small bubbles of air or other gas, such a froth may be used to fill the mold completely.
A further advantage of the use of a diazo thioether as a blowing agent in the process of this are vulcanization accelerators, and hence perform that function in addition to their role as blowing agents. The necessity of using additiona1 accelerators is thus eliminated. Diazo thioethers are also employed as initiators and modifiers in polymerization recipes,in the production of synthetic rubber. When synthetic rubber is produced from formulations in which diazo thioethers are employed, the diazo thioether already present may serve as a blowing agent in the manufacture of foam or sponge rubber, if it is present, as such, in the final polymer product in sufficient relative amount. In cases where an additional amount of this additive is considered desirable, such quantities as are necessary may be introduced prior to the blowing operation. If it is desired to produce an unvulcanized sponge rubber, the diazo thioether blowing agent may be admixed with raw rubber, without or with the concomitant admixture of other ingredients. This procedure can be used, for example, when nonvulcanizable synthetic rubber is to be blown. However, it is generally preferable to effect vulcanization of the rubber at the same time, and in invention lies in the fact that diazo thioethers such cases there is added, along with the diazo i 3 thioether blowing agent, the other ingredients which it is desired to incorporate in the rubber. In these instances, blowing and vulcanization oc cur together and the resulting sponge, foam, or cellular rubber product is also a vulcanized product. Since, as mentioned, diazo thioethers are vulcanization accelerators also, usual accelerators may be omitted, or used in less-than-normal amount. When a diazo thioether is used in very small concentration, its eflect as a vulcanization accelerator may exceed its effect as a blowing agent. i
Advantages of this invention areillustrated by the following examples. The reactants, and their proportions, and the other specific ingredients of the recipes are presented as being typical and should not be construed to limit the invention unduly Example I Compounding of a synthetic rubber base stock is effected according to the following recipe:
Parts by weight GR-S rubber stock Santocure 1 0.5 Calcined magnesia 4 Whiting 60 Carbon blackiPhilblack A) 15 Phenyl-beta-naphthylamine 2 Petroleum softener 20 Stearic acid r 2 Zinc oxide 5 '2- l-methoxybenzene diazo mercapto) naphthalene 3 1 N-cyclohexyl-2-benzothiazole sulfenamide.
When molds of suitable capacity are one-third to one-half filled with the compounded stock and heated at to C. under a steam pressure of 60 pounds per square inch gauge for 20 to 30 minutes, the molds are completely filled and the resulting products have fine, uniform pores and are firm but not harsh to the touch. Similar results are obtained when the diazo thioether employed is l-(4-methoxybenzene diazo mercapto) naphthalene.
$011 .22? zinc salt of an aryl mercaptan and 50% neutral 2 N,N"-diphenyl ethylenediamine.
Heating of the compounded material as in EX- ample I yields a soft sponge. Similar results are obtained when the diazo thioethers employed are 2- (4-methylbenzene diazo mercapto) -naphthalene and z-(zA-dimethylbenzene diazo, mercapto) -naphthalene, respectively.
Example. III
A firm sponge is prepared from a GR-S rubber stock by using the following compounding recipe:
2-( l-methoxybenzene diazo mercapto)- naphthalene 2 solvent.
2 l\,N-diphenyl cthylenediamine.
1 50% zinc salt of an aryl mercaptan and 50% neutral fieating' effected under conditions described in Example I. When 2-(4-methY-lbenzene diazo mercapto) -naphthalene and 2- (2,4-dimethylbenzene diazo mercapto) -naphthalene are'th'e diazo thioethers empioyed, comparable results are obtained. Similar results are also produced when 2-'-(4-'-chlorobenzene diazo mercaptoi-fz-methyl propane is used as the'blowing agent.
Example IV A natural rubber base stock-iscompounded according to the f'ollowingrecipe:
Parts by weight Smoked sheet 100 Zinc oxide g 5 Whiting 30 Phenyl-beta-naphthylamine 2 Santocure 1 0.5 Petroleum softener 20 Stearic acid l Sulfur 2 2 (4 methoxybenzene diazo mercapto)- naphthalene 1 N-cyc1ohexyl2-benzothiazole sulfenamide.
Foam rubber is prepared from -a sample of GR-S latex which is mechanically frothed, by intimatemixing with air, to about six times. its original volume and then admixed witha material comprising compounding, blowing, gelling, and vulcanizing ingredients. This latter material is prepared in the following manner:
Parts byweight Water 50] Phenyl-beta-naphthylamine :5 Piperidinium pentamethylene dithiocarbamate 4.5 Zinc oxide 20 Sulfur 10 Zinc mercaptobenzothiazole 5.5 Agerite white 6 1 Di-beta-naphthyl-para-phenylene diamine.
The water is heated to 80 to 85 C'., the phenylbeta-naphthylamine and piperidinium pentamethylene dithiocarbamate added, and the mixture placed in a ball mill after which the zinc oxide, sulfur, zinc mercaptobenzothiazole, and agerite white are introduced. The ingredients are milled until a uniform paste is obtained. In order to prevent foaming during the milling operation, the ball mill is filled to maximum capacity. To 100 parts of the paste is added parts of the sodium salt of 4-(4-sulfobenzene diazo mercapto)-toluene and 2.5 parts ammonium nitrate in the form of a 50 per cent aqueous solution. This mixture is stirred until a uniform dispersion is produced.
The compounding mixture prepared as described (2 parts) is added to 10 parts of latex frothed to about six times its original volume, and this mixture is poured into a mold which h'as been warmed to a temperature of 65 C. l The temperature. is increased to -90 C. to hasten gelling of the. latex and cause thefrothed rubber to expand and fill the mold completely. The slight pressure, caused by the freed gases, maintained until a-stiif gel is produced: after which the latex is vulcanized by heating the mold to.100 C.for about an hour.
TheGR-S rubber stock referred to some of the foregoing examples, is, as is well known to thoseskil-ledin the art, asynthetic rubber producedby emulsion copolymerization of a meme meric mixture of 1,3-butadiene (70-75%) and styrene (25-30%). This material was produced in. large quantities under government direction by'many organizations. As will be evident to those skilled in the art, various modifications of this invention can be made, orfollowed, in the light of the foregoing disclosure and discussion, without departing from the spirit or scope of the disclosure or from the scope of the claims. h
a I claim:
1. In the preparation of a blown rubber-product wherein there is admixed with the material from which the product is made a blowing agent which is decomposed in said material during the preparation of the product to cause an internal blowing efiect to aid in the formation of the product, the steps which comprise incorporating 0.5 to 10 per cent of a diazo thioether blowing agent in said material, said agent having the general formula R,N=NSR, wherein R is an aromatic radical and R is a member of the group consisting of aromatic, cycloalkyl and aliphatic radicals and then causing the decomposition of said agent. 7 r
2. In the preparation of a blown rubber product wherein there is admixed with the latex from which the product is made a glowing agent which is decomposed in said latex during the preparation of the product tocause an internal blowing effect to aid in the formation of the product, the steps which comprise incorporating 0.5 to 10 per-cent of a diazo thioether blowing'agent in said'latex, said agent having the general formula R-N:N-S-R', wherein R is an aromatic radical and It is a member of the group con-'- sisting of aromatic, cycloalkyl and aliphatic radicals and then causing the decomposition o said agent.
3. A process according to claim 2 wherein the latex is a synthetic latex.
4. A process according to claim 3 wherein the quantity of the diazo thioether incorporated is in the approximate range 0.5 to 10% by weight of the rubber in said latex and the admixture is heated to a temperature in the approximate range to 200 C. to cause the decomposition of said diazo thioether and for a time sufiicient to cause the formation of said product, said agent having the general formula R.-N=NS-R', wherein R is an aromatic radical and R is a member of the group consisting of aromatic, cycloalkyl and aliphatic radicals.
5. A process according to claim 4 wherein a froth is first formed by admixing a gas with said latex.
6. A process according to claim 2 wherein the latex is a natural latex.
'7. A process according to claim 6 wherein the quantity of the diazo thioether incorporated is in 'the'app'roximate range 0.5' to 10% by weight of the rubber in said latex and the admixture is heated to a temperature in the approximate range .90 to 200 C. to cause the decomposition of said diazo thioether and for a time suflicient to cause the formation of said product, said agent having the general formula R- :N-S-R', wherein R is an aromatic radical and R is a member vof the group consisting of aromatic, cycloalkyl and aliphaticradicals.
8. A process according to claim 7 wherein a froth is first formed by admixing a gas with said latex.
. :9; In the preparation of a blown rubber product wherein there is admixed with the rubber from which the product is made a blowing agent which is decomposed in said rubber during the preparation of the product to cause an internal blowing eifect to aid in the formation of the product, the steps which comprise incorporating 0.5 to 10 per cent of a diazo thioether blowing agent in said rubber, said agent having the general formula RN:NSR, wherein R is an aromatic radical and R is a member of the group consisting of aromatic, cycloalkyl and aliphatic radicals and then causing the decomposition of said agent.
10. A process according to claim 9 wherein the rubber is a synthetic rubber.
; 11. A process according to claim 10 wherein the quantity of the diazo thioether incorporated is in the approximate'range 0.5 to 10% by weight of the rubber and the admixture is heated to a temperature in the approximate range 90 to 200 C. to cause the decomposition of said diazo thioether and for a time sufficient to cause the formation of said product, said agent having the general formula R-N:NSR', wherein R is an aromatic radical and R is a member of the group consisting of aromatic, cycloalkyl and aliphatic radicals.
12. 'A process according to claim 9 wherein the rubber is a natural rubber.
13. A process according to claim 12 wherein the quantity of the diazo thioether incorporated is in the approximate range 0.5 to 10% by weight of the rubber and the admixture is heated to a temperature in the approximate range 90 to 200 C. to cause the decomposition of said diazo thioether and for atime suflicient to cause the formation of said product, said agent having the general formula RN:NSR', wherein R is an aromatic radical and R is a member of the 8 group consisting of aromatic, cycloalkyl and aliphatic radicals.
14. A process according to claim 1 wherein said diazo thioether is 2-(4-methoxybenzene diazo mercapto) -naphthalene.
15. A process according to claim 1 wherein said diazo thioether is 1-(4-methoxybenzene diazo mercapto) -naphthalene.
16. A process according to claim 1 wherein said diazo thioether is a 2,4-dimethylbenzene diazo mercapto-napthalene.
17. A process according to claim 1 wherein said diazo thioether is 2-(2,4-dimethylbenzene diazo mercapto) -naphthalene.
18. A process according to claim 9 wherein the rubber is a butadiene-styrene"synthetic rubber.
19. In the preparation of a blown product from a rubber selected from the group consisting of natural rubber and a butadiene-styrene rubber wherein there is admixed with the material from Which the product is made a blowing agent which is decomposed in said material during the'preparation of the product to cause an internal blow ing effect to aid in the formation of the product, the steps which comprise incorporating 0.5 to 10 per cent of a diazo thioether blowing agent in said material, said agent having the general formula RN:NSR', wherein R is an arcmatic radical and R is a member of the group consisting of aromatic, cycloalkyl and aliphatic radicals and causing the decomposition of said agent therein.
20. A process according to claim 1 wherein said diazo thioether is 2-(4-methylbenzene diazo mercapto) -naphthalene.
21. A process according to claim 1 wherein said diazo thioether mercapto) -2-methy1propane.
WILLIAM B. REYNOLDS.
References Cited in the file Of this patent UNITED STATES PATENTS Number Name Date 2,261,459 Cooper et a1 Nov. 4, 1941 2,284,578 Jones May 26, 1942 2,299,593 Roberts et al. Oct. 20, 1942 2,303,691 Harman Dec. 1, 1942 2,335,730 Blake Nov. 30, 1943 2,448,154 Richmond et al. Aug. 31, 1948 2,469,819 Flory et al. May 10, 1949 2,471,742 Harrison May 31, 1949 is 2- (4-chlorobenzene diazo

Claims (1)

1. IN THE PREPARATION OF A BLOWN RUBBER PRODUCT WHEREIN THERE IS ADMIXED WITH THE MATERIAL FROM WHICH THE PRODUCT IS MADE A BLOWING AGENT WHICH IS DECOMPOSED IN SAID MATERIAL DURING THE PREPARATION OF THE PRODUCT TO CAUSE AN INTERNAL BLOWING EFFECT TO AID IN THE FORMATION OF THE PRODUCT, THE STEPS WHICH COMPRISES INCORPORATING 0.5 TO 10 PER CENT OF A DIAZO THIOETHER BLOWING AGENT IN SAID MATERIAL, SAID AGENT HAVING THE GENERAL FORMULA R-N=N-S-R'', WHEREIN R. IS AN AROMATIC RADICAL AND R'' IS A MEMBER OF THE GROUP CONSISTING OF AROMATIC, CYCLOALKYL AND ALIPHATIC RADICALS AND THEN CAUSING THE DECOMPOSITION OF SAID AGENT.
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2819753A (en) * 1956-06-18 1958-01-14 Nogue Carlos Capella Method of making an inflated hollow rubber article
US2825747A (en) * 1954-10-01 1958-03-04 Du Pont Method for foaming rubber
US3192194A (en) * 1961-12-01 1965-06-29 Du Pont Diazothioether heterocyclic compounds
DE1245588B (en) * 1956-08-23 1967-07-27 Us Rubber Co Process for the production of sponge rubber
US3979353A (en) * 1975-04-15 1976-09-07 Westinghouse Electric Corporation Diazonium salt composition for forming thermoparticulating coating
US4016745A (en) * 1975-04-15 1977-04-12 Westinghouse Electric Corporation Monitoring electrical apparatus against overheating by the use of coating compositions containing thermoparticulatable diazonium salts
US4226945A (en) * 1977-03-05 1980-10-07 Henkel Kommanditgesellschaft Auf Aktien Rubber compositions expansible under vulcanization conditions
RU2655332C1 (en) * 2017-07-11 2018-05-25 Федеральное государственное бюджетное образовательное учреждение высшего образования "Волгоградский государственный технический университет" (ВолгГТУ) Method of volcanization of rubber mixture on the basis of natural rubber
RU2664070C1 (en) * 2017-07-11 2018-08-14 Федеральное государственное бюджетное образовательное учреждение высшего образования "Волгоградский государственный технический университет" (ВолгГТУ) Elastomer composition based on natural rubber

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US2261459A (en) * 1938-08-09 1941-11-04 American Cyanamid Co Process of manufacturing gas expanded structures
US2284578A (en) * 1939-06-30 1942-05-26 Goodrich Co B F Vulcanizable rubber compositions
US2299593A (en) * 1937-08-18 1942-10-20 Rubatex Products Inc Method of making closed cell expanded rubber by internally developed gases
US2303691A (en) * 1940-04-05 1942-12-01 Monsanto Chemicals Method of treating rubber
US2335730A (en) * 1940-11-09 1943-11-30 Monsanto Chemicals Sponge rubber
US2448154A (en) * 1947-10-18 1948-08-31 Us Rubber Co Use of symmetrical xenyltriazenes in making gas expanded organic plastics
US2469819A (en) * 1946-01-16 1949-05-10 Wingfoot Corp Vulcanization of rubber compositions
US2471742A (en) * 1946-07-13 1949-05-31 Goodrich Co B F Polymerization of acrylonitrile

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2299593A (en) * 1937-08-18 1942-10-20 Rubatex Products Inc Method of making closed cell expanded rubber by internally developed gases
US2261459A (en) * 1938-08-09 1941-11-04 American Cyanamid Co Process of manufacturing gas expanded structures
US2284578A (en) * 1939-06-30 1942-05-26 Goodrich Co B F Vulcanizable rubber compositions
US2303691A (en) * 1940-04-05 1942-12-01 Monsanto Chemicals Method of treating rubber
US2335730A (en) * 1940-11-09 1943-11-30 Monsanto Chemicals Sponge rubber
US2469819A (en) * 1946-01-16 1949-05-10 Wingfoot Corp Vulcanization of rubber compositions
US2471742A (en) * 1946-07-13 1949-05-31 Goodrich Co B F Polymerization of acrylonitrile
US2448154A (en) * 1947-10-18 1948-08-31 Us Rubber Co Use of symmetrical xenyltriazenes in making gas expanded organic plastics

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2825747A (en) * 1954-10-01 1958-03-04 Du Pont Method for foaming rubber
US2819753A (en) * 1956-06-18 1958-01-14 Nogue Carlos Capella Method of making an inflated hollow rubber article
DE1245588B (en) * 1956-08-23 1967-07-27 Us Rubber Co Process for the production of sponge rubber
US3192194A (en) * 1961-12-01 1965-06-29 Du Pont Diazothioether heterocyclic compounds
US3979353A (en) * 1975-04-15 1976-09-07 Westinghouse Electric Corporation Diazonium salt composition for forming thermoparticulating coating
US4016745A (en) * 1975-04-15 1977-04-12 Westinghouse Electric Corporation Monitoring electrical apparatus against overheating by the use of coating compositions containing thermoparticulatable diazonium salts
US4226945A (en) * 1977-03-05 1980-10-07 Henkel Kommanditgesellschaft Auf Aktien Rubber compositions expansible under vulcanization conditions
RU2655332C1 (en) * 2017-07-11 2018-05-25 Федеральное государственное бюджетное образовательное учреждение высшего образования "Волгоградский государственный технический университет" (ВолгГТУ) Method of volcanization of rubber mixture on the basis of natural rubber
RU2664070C1 (en) * 2017-07-11 2018-08-14 Федеральное государственное бюджетное образовательное учреждение высшего образования "Волгоградский государственный технический университет" (ВолгГТУ) Elastomer composition based on natural rubber

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